Mitochondrial biogenesis during cellular differentiation

Am J Physiol. 1997 Apr;272(4 Pt 1):C1345-51. doi: 10.1152/ajpcell.1997.272.4.C1345.


Mitochondrial biogenesis was studied during differentiation of two immortalized cell lines (C2C12, 3T3) with enzyme measurements, Northern blots, and quantitative ultrastructure. Citrate synthase, isocitrate dehydrogenase, and 3-hydroxyacyl-CoA dehydrogenase (nuclear encoded, mitochondrial matrix location) showed linear, four- to sixfold increases in enzymatic activity in C2C12 cells but increased exponentially in 3T3 cells. Cytochrome oxidase and NADH dehydrogenase (nuclear and mitochondrial encoded, cristae location) increased to a lesser extent and with a pattern dissimilar to the first group. Northern blots and activity of succinate dehydrogenase (cristae location but entirely nuclear encoded) suggested the groupings were based on location of the genes rather than the mature enzyme. However, quantitative electron microscopy and comparisons with adult tissue suggested that mitochondrial ultrastructure can influence the change in cristae enzymes. Cristae surface area per unit mitochondrial volume and per unit cell volume increased much less than did cristae enzymes. Available space on the inner membrane may become limiting and account for some aspects of the pattern of change in electron transport enzymes during differentiation.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 3T3 Cells
  • Animals
  • Cell Differentiation
  • Cell Line, Transformed
  • Enzymes / genetics
  • Fibroblasts / cytology*
  • Fibroblasts / enzymology
  • Fibroblasts / ultrastructure
  • Mice
  • Mitochondria / enzymology
  • Mitochondria / physiology*
  • Mitochondria / ultrastructure
  • Muscle, Skeletal / cytology*
  • Muscle, Skeletal / enzymology
  • Muscle, Skeletal / ultrastructure
  • RNA, Messenger / metabolism
  • Rats


  • Enzymes
  • RNA, Messenger